T27260 |
Emivirine
|
149950-60-7
|
99.68%
|
|
Emivirine (MKC-442) is a potent and selective nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1.
|
T0753 |
Salicylanilide
|
87-17-2
|
99.68%
|
|
Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.
|
TP1348 |
FC131 TFA (606968-52-9 free base)
|
842166-42-1
|
99.67%
|
|
FC131 TFA (606968-52-9 free base) (FC131 TFA) is an antagonist of CXCR4 that inhibits the binding of [125I] -sdf-1 to CXCR4(IC50 : 4.5 nM ), and has anti-hiv act...
|
T0100 |
Atazanavir sulfate
|
229975-97-7
|
99.67%
|
|
Atazanavir sulfate (BMS-232632 sulfate) is an azapeptide and HIV-PROTEASE INHIBITOR that is used in the treatment of HIV INFECTIONS and AIDS in combination with ...
|
T11074 |
Dolutegravir intermediate-1
|
1335210-23-5
|
99.67%
|
|
Dolutegravir intermediate-1 (1-(2,2-dimethoxyethyl)-5-methoxy-6-(methoxycarbonyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid) is a new synthetic Dolutegravir in...
|
T4578 |
Tipranavir
|
174484-41-4
|
99.66%
|
|
Tipranavir is a protease inhibitor that inhibits HIV-1 resistant to more than 1 protease inhibitor .Tipranavir effectively inhibits HIV-1 protease enzyme activit...
|
TN4673 |
(+)-Nortrachelogenin
|
61521-74-2
|
99.64%
|
|
(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.
|
T0194 |
Chloroquine phosphate
|
50-63-5
|
99.64%
|
|
Chloroquine phosphate (Aralen phosphate) is an aminoquinoline antimalarial and also is widely used as an autophagy inhibitor. Chloroquine also is an inhibitor of...
|
T4557 |
Amylmetacresol
|
1300-94-3
|
99.64%
|
|
Amylmetacresol (5-Methyl-2-Pentylphenol) is used in the treatment of sore throat or 'acute sore throat', pharyngitis, tonsillitis and laryngitis. As well as in t...
|
T6246 |
Cobicistat
|
1004316-88-4
|
99.62%
|
|
Cobicistat (GS-9350) is a carbamate and thiazole derivative that functions as a CYTOCHROME P450 CYP3A INHIBITOR to enhance the concentration of ANTI-HIV AGENTS, ...
|
T9039 |
HIV-1 Nef-IN-1
|
13728-56-8
|
99.62%
|
|
HIV-1 Nef-IN-1 is an inhibitor of HIV-1 Nef protein. It efficiently competes for Nef-SH3Hck interactions(Kd : 6.7 μM).
|
TN2158 |
Robinetin
|
490-31-3
|
99.61%
|
|
Robinetin (3,3',4',5',7-Pentahydroxyflavone) has antioxidant and antiradical activities, inhibits EYPC membrane lipid peroxidation and HbA glycosylation with hig...
|
T1595 |
Nevirapine
|
129618-40-2
|
99.6%
|
|
Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor. In combination with other antiretroviral drugs, nevirapine reduces HIV viral...
|
T8238 |
Fosamprenavir Calcium Salt
|
226700-81-8
|
99.59%
|
|
Fosamprenavir Calcium Salt (GW433908G) (GW433908G) is a phosphate ester prodrug of the antiretroviral protease inhibitor Amprenavir, with improved solubility. Fo...
|
T5782 |
Bevirimat
|
174022-42-5
|
99.58%
|
|
Bevirimat (PA-457) is a first-in-class inhibitor of HIV-1 maturation, blocking the cleavage of the Gag capsid (CA) precursor, CA-SPI, to mature CA protein during...
|
T7499 |
TAK-779
|
229005-80-5
|
99.58%
|
|
TAK-779 (Takeda 779) is an antagonist of chemokine receptor 5 (CCR5), CCR2b, and CXC chemokine receptor 3 (CXCR3).
|
T2551 |
Etravirine
|
269055-15-4
|
99.56%
|
|
Etravirine (R165335) is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor. Etravirine is designed to be active against HIV isolates with mutation...
|
T0984 |
5-Fluorouracil
|
51-21-8
|
99.56%
|
|
5-Fluorouracil (5-FU) is a uracil analog, an inhibitor of DNA synthesis. 5-Fluorouracil has antitumor activity and affects pyrimidine synthesis through inhibitio...
|
T0153 |
Oltipraz
|
64224-21-1
|
99.56%
|
|
Oltipraz (RP 35972) is a synthetic dithiolethione with potential chemopreventive and anti-angiogenic properties. Oltipraz induces phase II detoxification enzymes...
|
T10603 |
BRD-6929
|
849234-64-6
|
99.54%
|
|
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: 1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1....
|